| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43427483-43427603 | Rare:35 | ||||
| chr6:43427783-43427935 | Rare:44 | ||||
| chr6:43477415-43477739 | Common:1; Rare:84 | ||||
| chr6:43516727-43517168 | Common:6; Rare:161; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575797-43576240 | Common:2; Rare:171; Clinvar:8 | ||||
| chr6:43628832-43628952 | Rare:49 | ||||
| chr6:43629010-43629031 | Rare:5 | ||||
| chr6:43629035-43629593 | Common:3; Rare:160 | ||||
| chr6:43629988-43630189 | Common:1; Rare:43 | ||||
| chr6:43635755-43635914 | Common:1; Rare:46 | ||||
| chr6:43769934-43770266 | Common:8; Rare:82 | ||||
| chr6:43770444-43770472 | Rare:3 | ||||
| chr6:43770584-43770862 | Common:2; Rare:83; Clinvar:1 | ||||
| chr6:43771023-43771233 | Rare:81 | ||||
| chr6:43771669-43772053 | Common:4; Rare:69 |